Page last updated: 2024-10-18

homogentisic acid and Syndrome

homogentisic acid has been researched along with Syndrome in 2 studies

Homogentisic Acid: Dihydroxyphenylacetic acid with hydroxyls at the 2 and 5 positions of the phenyl ring.
homogentisic acid : A dihydroxyphenylacetic acid having the two hydroxy substituents at the 2- and 5-positions.

Syndrome: A characteristic symptom complex.

Research Excerpts

ExcerptRelevanceReference
"Alkaptonuria is a rare inherited disorder of tyrosine metabolism, which results in deposition of homogentisic acid in the connective tissues."3.79Choice of valve prosthesis in a rare clinical condition: aortic stenosis due to alkaptonuria. ( Cullen, H; Markman, P; Thakur, S, 2013)

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19901 (50.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's1 (50.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Thakur, S1
Markman, P1
Cullen, H1
Ritsner, MS1

Other Studies

2 other studies available for homogentisic acid and Syndrome

ArticleYear
Choice of valve prosthesis in a rare clinical condition: aortic stenosis due to alkaptonuria.
    Heart, lung & circulation, 2013, Volume: 22, Issue:10

    Topics: Aged; Alkaptonuria; Aortic Valve Stenosis; Heart Valve Prosthesis; Homogentisic Acid; Humans; Male;

2013
[Characteristics of tyrosine balance and oxidation in oligophrenia of different origin].
    Zhurnal nevropatologii i psikhiatrii imeni S.S. Korsakova (Moscow, Russia : 1952), 1977, Volume: 77, Issue:3

    Topics: Adolescent; Ascorbic Acid; Child; Female; Homogentisic Acid; Humans; Intellectual Disability; Male;

1977